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Compression Treatment Effects on Complications and Healing of Achilles Tendon Rupture

Primary Purpose

Rupture, Venous Thromboembolism, Venous Thrombosis

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Intermittent pneumatic compression (IPC)
Sponsored by
Karolinska University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Rupture focused on measuring Achilles Tendon, Immobilization, Wound Healing, Intermittent Pneumatic Compression, Ultrasonography, Microdialysis

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Achilles tendon rupture operated on within 96 hours of diagnose.

Exclusion Criteria:

  1. Inability or refusal to give informed consent for participation in the study
  2. Ongoing treatment with anticoagulant therapy
  3. Inability to comply with the study instructions
  4. Known kidney disorder
  5. Heart failure with pitting oedema
  6. Thrombophlebitis
  7. Recent thromboembolic event (during the preceding 3 months)
  8. Recent surgery (during the preceding month)
  9. Presence of known malignancy
  10. Current bleeding disorder
  11. Pregnancy

Sites / Locations

  • Karolinska University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Routine care: Plaster Cast Treatment

Intermittent pneumatic compression (IPC)

Arm Description

Two weeks of postoperative conventional lower limb plaster cast immobilization in 30 degrees of plantarflexion

Two weeks of calf IPC by Aircast® VenaFlow® Elite System during immobilization in an orthosis Aicast® XP Walker.

Outcomes

Primary Outcome Measures

Venous Thromboembolic Events (VTE)
At 2 weeks postoperatively the number of participants with VTE events will be assessed by: 1) DVT detected by compression duplex ultrasound (CDU) , 2) isolated calf muscle vein thrombosis (ICMVT) detected by CDU, 3) symptomatic DVT or ICMVT detected by CDU, 4) symptomatic pulmonary embolism detected by computer tomography.

Secondary Outcome Measures

Functional Outcome - Muscular Endurance Tests (Heel-rise)
The functional outcome was assessed at 1year post-operatively by the validated calf muscle endurance test, i.e. heel rise test (Silbernagel KG et al. A new measurement of heel-rise endurance with the ability to detect functional deficits in patients with Achilles tendon rupture. Knee Surg Sports Traumatol Arthrosc. 2010). The Muscle lab linear encoder (Ergotest Technology, Oslo, Norway), was used for data collection. Standardized footwear was used. Patients warmed up before testing. During the heel-rise test, verbal encouragement was used. The patient was instructed to go as high as possible on each heel-rise with a straight knee. A metronome was used for standardized frequency of 30 heel-rises per minute. The test was terminated when the patient stopped or could not maintain frequency. For analysis, the limb symmetry index (LSI, percentage of injured vs. uninjured side) values were used.
Venous Thromboembolic Events (VTE)
At 6 weeks postoperatively the number of participants with VTE events will be assessed by: 1) DVT detected by compression duplex ultrasound (CDU) , 2) isolated calf muscle vein thrombosis (ICMVT) detected by CDU, 3) symptomatic DVT or ICMVT detected by CDU, 4) symptomatic pulmonary embolism detected by computer tomography.
Patient-reported Outcome
The patients' symptoms will be assessed using the Achilles tendon Total Rupture Score (0-100, 100=best)
Microdialysis
At 2 weeks postoperatively in-vivo microdialysis will be performed on as described by Greve et al 2012 (DOI: 10.1111/j.1600-0838.2012.01475.x). In the microdialysate substances will be assessed, eg. markers of tendon callus production, procollagen type I (PINP), by enzymatic quantification.
Time From Injury to Surgery
Prognostic factor: Time to surgery , i.e. the time from ATR injury to start of the surgical procedure, will be calculated by using the time-point at which the patient sustained the injury as described in the patient journal, as well as the starting time point of the surgery as registered in the computerized operation report.

Full Information

First Posted
March 16, 2011
Last Updated
October 5, 2023
Sponsor
Karolinska University Hospital
Collaborators
Region Stockholm, DJO Incorporated
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1. Study Identification

Unique Protocol Identification Number
NCT01317160
Brief Title
Compression Treatment Effects on Complications and Healing of Achilles Tendon Rupture
Official Title
Intermittent Pneumatic Compression Effects on Venous Thromboembolism Incidence and Healing of Achilles Tendon Rupture
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
September 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska University Hospital
Collaborators
Region Stockholm, DJO Incorporated

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This prospective randomized study aims to determine whether intermittent pneumatic compression (IPC), 75 patients, beneath functional bracing compared to treatment-as-usual in plaster cast, 75 patients, can reduce the Venous Thromboembolism (VTE) incidence and promote healing of sutured acute Achilles tendon ruptures. At two weeks post surgery, the IPC intervention will be ended and both patient groups will be immobilized in an orthosis until follow-up at six weeks. The endpoint of the first part of the study is VTE events. The primary outcome will be the DVT-incidence at two weeks, assessed using screening compression duplex ultrasound (CDU) by two ultrasonographers masked to the treatment allocation. Secondary outcome will be the DVT-incidence at 6 weeks. 1) Deep Vein Thrombosis (DVT) detected by CDU , 2) isolated calf muscle vein thrombosis (ICMVT) detected by CDU, 3) symptomatic DVT or ICMVT detected by CDU, 4) symptomatic pulmonary embolism detected by computer tomography. The endpoint of the second part of the study is tendon healing quantified at 2 weeks by microdialysis followed by quantification of markers for tendon repair. The endpoint of the third part of the study is the functional outcome of the patients at one year post-operatively using four reliable and valid scores, i.e. the Achilles tendon Total Rupture Score (ATRS), Physical Activity scale (PAS), Foot and Ankle Outcome Score (FAOS) and EuroQol Group's questionnaire (EQ-5D) as well as the validated heel-rise test.
Detailed Description
The incidence of DVT after Achilles tendon rupture is as high as 30-40% and patients exhibit a prolonged healing process with variable outcome. Moreover, it has been demonstrated that low molecular weight heparin had no effect on preventing DVT after Achilles tendon surgery. Whether intermittent pneumatic compression (IPC) can prevent DVTs and improve healing after Achilles tendon rupture has to our knowledge not been tested before.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rupture, Venous Thromboembolism, Venous Thrombosis, Surgical Wound Infection
Keywords
Achilles Tendon, Immobilization, Wound Healing, Intermittent Pneumatic Compression, Ultrasonography, Microdialysis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Routine care: Plaster Cast Treatment
Arm Type
No Intervention
Arm Description
Two weeks of postoperative conventional lower limb plaster cast immobilization in 30 degrees of plantarflexion
Arm Title
Intermittent pneumatic compression (IPC)
Arm Type
Experimental
Arm Description
Two weeks of calf IPC by Aircast® VenaFlow® Elite System during immobilization in an orthosis Aicast® XP Walker.
Intervention Type
Device
Intervention Name(s)
Intermittent pneumatic compression (IPC)
Other Intervention Name(s)
VenaFlow Elite system, VenaFlow® System
Intervention Description
6 hours IPC, daily, applied to both calves during two weeks post-operatively. The VenaFlow Elite system (Aircast, Vista, California) uses calf cuffs containing two overlapping air chambers located posteriorly on the leg. As the device cycles, the distal chamber inflates to 52 mm Hg over half a second. During the last 0.2 second of this period, the proximal chamber inflates and reaches 45 mm Hg. After six seconds of inflation the cuff deflates, and the cycle is repeated every minute.
Primary Outcome Measure Information:
Title
Venous Thromboembolic Events (VTE)
Description
At 2 weeks postoperatively the number of participants with VTE events will be assessed by: 1) DVT detected by compression duplex ultrasound (CDU) , 2) isolated calf muscle vein thrombosis (ICMVT) detected by CDU, 3) symptomatic DVT or ICMVT detected by CDU, 4) symptomatic pulmonary embolism detected by computer tomography.
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Functional Outcome - Muscular Endurance Tests (Heel-rise)
Description
The functional outcome was assessed at 1year post-operatively by the validated calf muscle endurance test, i.e. heel rise test (Silbernagel KG et al. A new measurement of heel-rise endurance with the ability to detect functional deficits in patients with Achilles tendon rupture. Knee Surg Sports Traumatol Arthrosc. 2010). The Muscle lab linear encoder (Ergotest Technology, Oslo, Norway), was used for data collection. Standardized footwear was used. Patients warmed up before testing. During the heel-rise test, verbal encouragement was used. The patient was instructed to go as high as possible on each heel-rise with a straight knee. A metronome was used for standardized frequency of 30 heel-rises per minute. The test was terminated when the patient stopped or could not maintain frequency. For analysis, the limb symmetry index (LSI, percentage of injured vs. uninjured side) values were used.
Time Frame
one year
Title
Venous Thromboembolic Events (VTE)
Description
At 6 weeks postoperatively the number of participants with VTE events will be assessed by: 1) DVT detected by compression duplex ultrasound (CDU) , 2) isolated calf muscle vein thrombosis (ICMVT) detected by CDU, 3) symptomatic DVT or ICMVT detected by CDU, 4) symptomatic pulmonary embolism detected by computer tomography.
Time Frame
6 weeks
Title
Patient-reported Outcome
Description
The patients' symptoms will be assessed using the Achilles tendon Total Rupture Score (0-100, 100=best)
Time Frame
One year
Title
Microdialysis
Description
At 2 weeks postoperatively in-vivo microdialysis will be performed on as described by Greve et al 2012 (DOI: 10.1111/j.1600-0838.2012.01475.x). In the microdialysate substances will be assessed, eg. markers of tendon callus production, procollagen type I (PINP), by enzymatic quantification.
Time Frame
2 weeks
Title
Time From Injury to Surgery
Description
Prognostic factor: Time to surgery , i.e. the time from ATR injury to start of the surgical procedure, will be calculated by using the time-point at which the patient sustained the injury as described in the patient journal, as well as the starting time point of the surgery as registered in the computerized operation report.
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Surgeon Sex
Description
Prognostic factor: All patients are operated on according to a standardized surgical protocol. and the surgeon on duty will perform the surgical repair and no specific surgeon can be selected by the patients. Unknown sex of the operating surgeon will be included as an additional exclusion criterion in the study.
Time Frame
Surgery will be performed within 10 days of injury
Title
Surgeon Experience
Description
Prognostic factor: All patients are operated on according to a standardized surgical protocol. and the surgeon on duty will perform the surgical repair and no specific surgeon can be selected by the patients. The experienced group of surgeons will consist of specialists accredited with a specialist licence issued by The Swedish National Board of Health and Welfare. The less experienced group of surgeons will consist of residents.
Time Frame
Surgery will be performed within 10 days of injury

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Achilles tendon rupture operated on within 96 hours of diagnose. Exclusion Criteria: Inability or refusal to give informed consent for participation in the study Ongoing treatment with anticoagulant therapy Inability to comply with the study instructions Known kidney disorder Heart failure with pitting oedema Thrombophlebitis Recent thromboembolic event (during the preceding 3 months) Recent surgery (during the preceding month) Presence of known malignancy Current bleeding disorder Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul W Ackermann, MD, PhD
Organizational Affiliation
Karolinska University Hospital, 171 76 Stockholm, SWEDEN
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
17176
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Plan to share data on primary outcome (DVT)
IPD Sharing Time Frame
Starting 12 months after publication the data will be available for 10 years after the study is published.
IPD Sharing Access Criteria
Contact PI.
Citations:
PubMed Identifier
25922463
Citation
Domeij-Arverud E, Labruto F, Latifi A, Nilsson G, Edman G, Ackermann PW. Intermittent pneumatic compression reduces the risk of deep vein thrombosis during post-operative lower limb immobilisation: a prospective randomised trial of acute ruptures of the Achilles tendon. Bone Joint J. 2015 May;97-B(5):675-80. doi: 10.1302/0301-620X.97B5.34581.
Results Reference
result
PubMed Identifier
28668970
Citation
Abdul Alim M, Domeij-Arverud E, Nilsson G, Edman G, Ackermann PW. Achilles tendon rupture healing is enhanced by intermittent pneumatic compression upregulating collagen type I synthesis. Knee Surg Sports Traumatol Arthrosc. 2018 Jul;26(7):2021-2029. doi: 10.1007/s00167-017-4621-8. Epub 2017 Jul 1.
Results Reference
result
PubMed Identifier
35596679
Citation
Chen J, Wang J, Hart DA, Ahmed AS, Ackermann PW. Complement factor D as a predictor of Achilles tendon healing and long-term patient outcomes. FASEB J. 2022 Jun;36(6):e22365. doi: 10.1096/fj.202200200RR.
Results Reference
derived
PubMed Identifier
30169112
Citation
Svedman S, Juthberg R, Edman G, Ackermann PW. Reduced Time to Surgery Improves Patient-Reported Outcome After Achilles Tendon Rupture. Am J Sports Med. 2018 Oct;46(12):2929-2934. doi: 10.1177/0363546518793655. Epub 2018 Aug 31.
Results Reference
derived
PubMed Identifier
27900179
Citation
Alim MA, Svedman S, Edman G, Ackermann PW. Procollagen markers in microdialysate can predict patient outcome after Achilles tendon rupture. BMJ Open Sport Exerc Med. 2016 Jun 10;2(1):e000114. doi: 10.1136/bmjsem-2016-000114. eCollection 2016.
Results Reference
derived

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Compression Treatment Effects on Complications and Healing of Achilles Tendon Rupture

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